Substrate-reactive coating composition

ABSTRACT

Crosslinkable aqueous-based coating compositions are described which are covalently bonded to a wooden surface to which they are applied. The compositions contain a crosslinkable polymer, a mono and/or polyethylenically unsaturated monomer which can be graft polymerized onto cellulose molecules present in said wooden surface, a water soluble peroxy free radical polymerization catalyst, a source of cations capable of creating free radical sites in said cellulose molecules and, optionally, a crosslinking agent for said crosslinkable polymer. The coating may be air dried under ambient conditions to provide a crosslinked coating which is chemically bonded to the underlying wooden surface.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention relates to curable coating compositions for substratessuch as wood which are chemically bonded to the substrate.

2. Description of Related Art

It is generally known in the art that the surface properties of shapedarticles such as polymeric films and fibers can be modified by graftpolymerization processes wherein the article is treated with a freeradical generating agent such as an organic peroxide or high energyradiation and then contacted with an ethylenically unsaturated monomericmaterial under conditions wherein the monomer or graft polymer chain iscaused to be covalently bonded to the substrate.

One particular process involves the treatment of natural or syntheticpolymer substrates containing active hydrogen with an aqueous solutioncontaining a silver salt (silver nitrate), a free radical polymerizationcatalyst and a free radically polymerizable monomer. The silver saltacts upon the substrate to remove active hydrogen thereby creatingactive sites or free radicals along the molecular chain and initiatingand propagating polymerization of the monomer in conjunction with thefree radical polymerization catalyst. The resulting product is a graftcopolymer comprising a substrate having a plurality of polymeric sidechains covalently bonded thereto. Examples of such processes aredisclosed in U.S. Pat. Nos. 3,401,049 and 3,698,931.

Although cellulose or wood is a substrate whose surface properties maybe modified in accordance with the disclosure of the above referencedpatents, this technology has not heretofore found application as meansof providing a protective coating for wood products. The durability andweatherability of wood is limited because it is highly hydrophilic andis subject to attack by water, fungi and bacteria, particularly inoutdoor applications. It is thus necessary to "seal" the wood by theapplication of protective coatings which form a barrier between the woodand the elements. The mere formation of grafted side chains on woodsurfaces does not provide the degree of barrier protection needed tosignificantly prolong the life of the wood.

Typical protective coatings for wood include linseed oil, acrylic orpolyurethane based paints and lacquers. However, these coatings aresusceptible to abrasion, UV deterioration oxidation and permeation bymoisture which limits their useful lifetime, particularly in outdoorapplications. Also, adhesion to the wooden substrate may quicklydeteriorate as a result of permeation by water, chemical attack, mildew,fungi and other causes.

Organic solvent-based coating compositions are known in the art based oncompositions curable by condensation reactions and containing polymericmaterial such as hydroxy terminated polyesters, diesters, acrylics andalkyds and an amino or polyisocyanate crosslinking agent. Theseformulations are adapted to be applied to a substrate such as metal,heated to drive off the solvent and further heated at temperatures above80° C. to activate the crosslinking mechanism. As such, these protectivecoatings find few practical applications on wood substrates because ofthe necessity to employ heat to activate the crosslinking mechanism. Anexample of a coating which is curable by condensation and free radicalreactions is found in U.S. Pat. No. 5,087,690.

Wood coating formulations which can be cured without heat are also knownin the art. For example, U.S. Pat. No. 4,171,387 discloses protectiveand decorative coatings for cellulose (wood) substrates based on apolyurethane base coat applied as a solution in organic solvent, whichis further overcoated with an ultraviolet curable polyacrylic resincontaining a photo-initiator. However, such coatings are also of limitedinterest due to the need to expose the coated surface to ultravioletradiation to cure the composition.

Other coating formulations which may be cured at ambient or elevatedtemperatures are disclosed in U.S. Pat. No. 4,303,563. These are organicsolvent based formulations containing an addition polymer which includespendant primary or secondary amine groups and, as a crosslinkingcomponent, one or a mixture of monomers or prepolymers containing atleast two unsaturated acryloxy groups.

Despite these developments, there exists a need to develop coatings,particularly coatings for wood, which can be cured at ambienttemperatures, can be formulated without added organic solvents and whichexhibit good initial and prolonged adhesion to the substrate and sealthe substrate.

SUMMARY OF THE INVENTION

The present invention provides a reactive coating formulation for woodand other substrates in the form of an aqueous dispersion whichcomprises a mixture of:

a) a water dispersible polymer containing reactive functionalityselected from the group consisting of hydroxy, epoxy, amide, carboxy andisocyanate functionality;

b) at least one mono- or polyethylenically unsaturated monomer;

c) an at least partially water soluble peroxy free radicalpolymerization catalyst; and

d) a source of cations selected from the group consisting of Ce⁴, Ce³,Fe³, Fe², CO², Cu² and Ag¹.

The composition also may contain a crosslinking agent for said waterdispersible polymer and other ingredients commonly present in paint andlacquer formulations.

The coating compositions of the invention are designed such that, uponapplication to cellulose wood substrates or other substrates containingactive hydrogen, a chemical reaction takes place wherein theethylenically unsaturated monomer is grafted onto the substrate to forma single "mer" unit or a grafted side chain containing a plurality ofpolymerized "mer" units. These grafted units contain functional groupsor ethylenically unsaturated groups which further react by ionic or freeradical crosslinking reactions to produce a crosslinked coating which isattached to the underlying substrate by covalent bonds.

DESCRIPTION OF THE INVENTION

Monoethylenically unsaturated monomers which are suitable as componentsin the composition of this invention include those which containhydroxy, carboxy or amino functionality. Examples of suitable monomersinclude acrylonitrile or methacrylonitrile, acrylamide ormethacrylamide, N-vinyl caprolactam, N-vinyl carbazole, maleicanhydride, itaconic acid, vinyl acetate and like materials and mixturesthereof. Particularly preferred monoethylenically unsaturated monomersare acrylic acids and esters responding to the formula ##STR1## whereinR is either hydrogen or C₁ or C₄ alkyl and R₁ is selected from the groupconsisting of hydrogen, alkyl, aminoalkyl, hydroxyalkyl, hydroxyalkoxyand cycloalkyl groups having from 1 to about 20 carbon atoms. Examplesof such monomers include acrylic or methacrylic acid, methyl acrylate ormethacrylate, ethyl acrylate or methacrylate, butyl acrylate ormethacrylate, hexyl or cyclohexyl acrylate or methacrylate, 2-ethylhexylacrylate or methacrylate, hydroxyethyl or hydroxypropyl acrylate ormethacrylate, dimethylaminoethyl acrylate or methacrylate, and alkyleneglycol or polyalkylene glycol mono acrylates or methacrylates such asethylene glycol acrylate or methacrylate, propylene glycol acrylate ormethacrylate, polyethylene glycol acrylate or methacrylate,polypropylene glycol acrylate or methacrylate and like materials andmixtures thereof. The above monomers containing functional groups may beused in mixture with other monomers such as styrene, alpha-methylstyrene, vinyl or vinylidene chloride, vinyl ethers and the like tofurther modify the properties of the coating composition.

Polyethylenically unsaturated monomers which may be used in the coatingcomposition include divinyl benzene, diallyl chloromethyl phosphonate,diallylbenzene phosphonate, diallyl dimethyl ammonium chloride and likematerials and mixtures thereof. Particularly preferred of such monomersare acryloyl compounds having the structure: ##STR2## wherein R₂ ishydrogen or C₁ -C₂ alkyl, n is 2, 3 or 4 and Z is the residuum of apolyol having from 2 to about 20 carbon atoms. Examples of suitable suchmonomers include ethylene glycol di(meth) acrylate, polyethylene glycoldi(meth) acrylate, diethylene glycol di(meth) acrylate, propylene glycoldi(meth) acrylate, polypropylene glycol di(meth) acrylate, trimethyleneglycol di(meth) acrylate, neopentyl glycol di(meth) acrylate,1,3-butylene glycol di(meth) acrylate, 1,4-butylene glycol di(meth)acrylate, 1,6-hexamethylene glycol di(meth) acrylate, 1,10-decamethyleneglycol di(meth) acrylate, trimethylolpropane tri(meth) acrylate,pentaerythritol tetra (meth) acrylate, pentaerythritol tri(meth)acrylate, alkoxlated versions of the above and like materials, as wellas mixtures thereof.

Mixtures of one or more of the above monoethylenically unsaturatedmonomers and one or more of the above polyethylenically unsaturatedmonomers may also be used, e.g., a mixture of hydroxyethyl acrylate andpolyethylene glycol di(meth) acrylate.

The composition also contains a graft polymerization initiator whichfunctions to abstract an active hydrogen atom from the molecules ofsubstrate materials, e.g. wood or cellulose, to which the coatingcomposition is applied, thereby creating a number of free radical sitesalong the molecular chains which serve as grafting sites for theunsaturated monomers present in the composition. In cellulosic materialssuch as wood, these active hydrogen atoms are present in the methylol(CH₂ OH) groups which are pendant from the molecules; in polyamidepolymer substrates the active hydrogen is the amido hydrogen; and inpolypropylene polymer substrates the active hydrogen is attached to thecentral carbon atom of the three carbon atom propylene molecules.Creation of these radicals serves to initiate polymerization of theunsaturated monomer under ambient conditions, which is furtherpropagated using a free radical polymerization catalyst.

Suitable graft polymerization initiators which are present in thecomposition include organic or inorganic salts of metals whichdissociate in the presence of water to provide cations selected from thegroup consisting of Ce⁴, Ce³, Fe³, Fe², Co², Cu² and Ag¹. Such saltsinclude the acetates, sulfates, perchlorates, carbonates and nitrates.Silver nitrate is an especially preferred source of ions because it alsohas the serendipitous function of imparting bactericidal and fungicidalproperties into the composition.

An at least partially water soluble peroxy free radical polymerizationcatalyst is also present in the composition. This catalyst is activatedby the metal ion radical and serves to propagate graft polymerization atambient conditions. Preferred catalysts include hydrogen peroxide, ureaperoxide, peracetic acid, ammonium persulfate and potassium persulfate.Urea peroxide is the more preferred catalyst.

The mechanism for the graft reaction onto performed substrates usingthese reagents is more completely disclosed in U.S. Pat. Nos. 3,401,049and 3,698,931, the complete disclosures of which are incorporated hereinby reference.

The major component present in the composition of this invention is awater dispersible polymer or prepolymer containing reactivefunctionality selected from the group consisting of hydroxy, epoxy,amide, carboxy and isocyanate functionality. Typical of such polymersare acrylic polymer emulsions which are copolymers of one or more alkylacrylates or methacrylates or mixtures thereof with ethylenicallyunsaturated monomers containing hydroxy, epoxy, amide, carboxy orisocyanate functionality, such as acrylic or methacrylic acid,acrylamide or methacrylamide or hydroxy-containing monomers such as ahydroxy alkyl acrylate or methacrylate, and allylalcohols. Typical ofsuch acrylic polymers are copolymers and terpolymers containing one or amixture of C₁ to C₈ alkyl acrylates or methacrylates such as methyl(meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate,ethylhexyl (meth) acrylate and the like with up to about 10 wt % of afunctional acrylic monomer such as (meth) acrylic acid,hydroxyethyl(meth)acrylate or (meth)acrylamide.

Typical urethane polymers or prepolymers containing isocyanatefunctionality include water dispersible reaction products of an organicpolyisocyanate such as toluene diisocyanate, hexamethylene diisocyanate,4,4-diphenylmethane diisocyanate, 1,3-cyclopentylene diisocyanate andlike materials with a polyol (diol, triol, tetrol) containing activehydrogen such as ethylene glycol, diethylene glycol, propylene glycol,neopentyl glycol, butane triol, pentaerythritol, mannitol, polyethyleneglycol, polypropylene glycol and epoxidized oils.

Hybrid water dispersible prepolymers containing (meth) acryloylfunctionality are also useful in the present invention. These areprepared by reaction of an acryloxy-containing compound such as (meth)acrylic acid, (meth) acryl halide, or a (meth) acrylic acid ester withvarious compounds such as hydroxy-containing alkyd resins, polyestercondensates, polyisocyanates or polyether condensates. Examples includematerials such as:

(A) Urethane acrylates obtained by reacting isocyanate groups ofpolyisocyanate, such as hexamethylene diisocyanate with a hydroxyalkylacrylate, e.g. hydroxyethyl acrylate. These polyurethane polyacrylatemonomers are disclosed in U.S. Pat. No. 3,297,745.

(B) Polyether acrylates obtained by esterification of hydroxy-terminatedpolyethers with acrylic acid as disclosed in U.S. Pat. No. 3,380,831.

(C) Polyesters having at least two acrylate groups obtained byesterifying hydroxyl groups with acrylic acid as disclosed in U.S. Pat.No. 3,935,173.

(D) Polyfunctional acrylates disclosed in U.S. Pat. No. 3,560,237, e.g.obtained by reaction of a hydroxyalkyl acrylate, e.g. hydroxyethylacrylate, with any one of:

(a) Dicarboxylic acids having from 4 to 15 carbon atoms,

(b) Polyepoxides having terminal glycidyl groups,

(c) Polyisocyanates having terminal reactive isocyanate groups.

(E) Acrylate-terminated polyesters made from acrylic acid, a polyolhaving at least three hydroxyl groups, and a dicarboxylic acid (U.S.Pat. No. 3,567,494).

(F) Polyacrylates obtained by the reaction of acrylic acid with at leasttwo epoxy groups of epoxidized drying oils, such as soybean oil, linseedoil, and the like, e.g. epoxidized corresponding drying oil fatty acid,an ester or amide thereof, or the corresponding alcohol, containing atleast 2 epoxy groups. Such polyfunctional acrylates are disclosed inU.S. Pat. No. 3,125,592.

(G) Polyacrylates which are urethane or amine derivatives of thepolyacrylated epoxidized drying oils, fatty acids and the likedescribed-in (F), obtained by the reaction of isocyanate(s) or amine(s)respectively with the polyacrylated epoxidized drying oils, fatty acids,and the like described in U.S. Pat. No. 3,125,592. The urethane andamine derivatives retain some or all of the acrylate groups and aredisclosed in U.S. Pat. Nos. 3,876,518 and 3,878,077.

(H) Polyacrylates obtained by reaction of acrylic acid by addition tothe epoxy groups of aromatic bisphenol-based epoxy resins as disclosedin U.S. Pat. No. 3,373,075.

(I) Polyacrylates obtained by the addition of acrylic acid to a linearvinyl polymer having pendant glycidyl groups, e.g. polymers of glycidylacrylate or of vinyl glycidyl ether or vinyl glycidyl sulfide asdisclosed in U.S. Pat. No. 3,530,100.

(J) Polyfunctional acrylates derived from acrylic acid anyhydride andpolyepoxides as disclosed in U.S. Pat. No. 3,676,398.

(K) Polyfunctional acrylate urethane esters obtained from the combiningof hydroxyalkyl acrylates, a diisocyanate, and a hydroxyl functionalalkyd condensate as disclosed in U.S. Pat. No. 3,673,140.

(L) Acrylate terminated urethane polyesters obtained by reaction of apolycaprolactone diol or triol with an organic polyisocyanate, e.g. adiisocyanate, and a hydroxyalkyl acrylate. Such products are disclosedin U.S. Pat. No. 3,700,643.

(M) Urethane polyacrylates obtained by reaction of a hydroxyl-containingester of a polyol with acrylic acid and a polyisocyanate, such as thosedescribed in U.S. Pat. No. 3,759,809.

These polymers contain functional groups which are capable of eitherreacting or interacting with functional groups present in the graftcopolymer side chains covalently attached to the coated substrate toform ionic or hydrogen bonds, or they contain unsaturated groups whichmay participate in the free radical polymerization reaction to provide acrosslinked polymer network.

Where the polymeric component contains functional groups which arecapable of undergoing ionic condensation reactions, e.g., carboxy,hydroxy or epoxy functionality, the composition may also includeeffective amounts of a crosslinking agent. Suitable crosslinking agentsinclude melamine based amino resins such as hexamethoxymethylmelamine,benzoguanamine resins, urea formaldehyde resins, glycoluryl-based resinsand like materials. Preferred crosslinking agents are those which areactive at ambient temperatures, i.e., 20°-30° C., and include epoxysilanes such as gamma glycidoxypropyltrimethoxy silane,beta-(3,4-epoxycyclohexyl) ethyltrimethoxy silane and polyfunctionalaziridines. A preferred aziridine is a 1-aziridinepropanoic acid,2-methl-, 2ethyl-2-[(3-(2-methyl-1-aziridinyl)-1-oxypropoxy]methyl)-1,3-propandiylester marketed by ICI Resins, Inc. under the tradename CX-100.

The composition of this invention may also include other ingredients inamounts which are commonly included in paint and lacquer formulationssuch as pigments, pigment extenders, wetting agents, surfactants,bactericides, fungicides, mildewicides, emulsifiers, suspending agents,flow control agents such as waxes or wax dispersions, level agents,thickening agents, pH control agents, slip agents such as silica or clayand the like.

Suitable pigments which may be included in the compositions of thisinvention are those opacifying pigments normally used in paint andcoating formulations and include titanium dioxide, zirconium oxide,zircon, zinc oxide, iron oxide, antimony oxide, carbon black, as well aschrome yellows, greens, oranges and the like. Preferred pigments includerutile TiO₂ and particularly weather resistant coated types of TiO₂. Thepigments may also be blended with a suitable extender material whichdoes not contribute significantly to hiding power. Suitable extendersinclude silica, baryte, calcium sulfate, magnesium silicate (talc),aluminum oxide, aluminum silicate, calcium silicate, calcium carbonate(mica), potassium aluminum silicate and other clays or clay-likematerials. Where present, the pigments and extenders are normallypresent at a level of from about 0.1 to about 1.0 parts by weight perpart by weight of the polymer components of the composition, on a dryweight basis.

The major organic component of the composition is the polymer orprepolymer component (a) which may be present at a level of from about35 to about 95% by weight, on a dry weight basis, more preferably fromabout 50 to about 90% by weight. These polymers and prepolymers areformulated into the composition as water-based or water misciblesolvent-based emulsions or dispersions containing the polymer componentat a level generally in the range of from about 20 to about 45% byweight solids.

The mono-or polyethylenically unsaturated component (b) may be presentin the dispersion at a level of from about 0.05 to about 5% by weight,more preferably from about 0.1 to about 2.5% by weight, based on theweight of the aqueous dispersion.

The concentration of the peroxy free radical catalyst component (c)added to the composition may generally range from about 0.0001 to about0.1% by weight based on the weight of the aqueous dispersion, and isadded to the composition preferably as a dilute solution in water.

The concentration of the metal salt component (d) may range from about0.01 to 0.0001% by weight of the aqueous dispersion. It is preferablyadded at a level sufficient to provide from about 10 to about 100 ppm ofdissociated cation species based on the weight of the aqueousdispersion.

The amount of the crosslinking component added to the composition mayrange from about 1 to about 15% by weight per 100 parts by weight ofsaid water dispersible polymer, on a dry weight basis. The preferredlevel of addition is a stoichiometric level of from about 0.25 to about2.0 equivalents, preferably about 1 equivalent, per equivalent ofreactive functional groups present in the water dispersible polymer.

The components may be mixed by adding the monomers, free radicalcatalyst, graft initiator and other ingredients to the aqueous polymeremulsion or dispersion and stirring to obtain a uniform mixture. Wherethe composition includes a pigment, it is preferably added as an aqueousor acrylic polymer dispersion. Otherwise, the pigment should be added tothe dispersion under high shear mixing conditions to insure a uniformdispersion of the pigment in the aqueous vehicle.

The pH of the formulated coating composition should preferably be in therange of from about 6-8, and appropriate amounts of a suitable acid,e.g. phosphoric or acetic acids or a base, e.g. sodium hydroxide,ammonia or ammonium hydroxide, may be included into the composition toadjust the pH as necessary.

The coating composition also preferably includes one or more surfactantsor wetting agents which may be ionic or non-ionic in character. Thepresence of a wetting agent is particularly desirable to reduce surfacetension and ensure uniform contact with the substrate. Where present, itis normally included at a level of from about 0.5 to about 10% by weightof the aqueous dispersion.

Where the composition includes a crosslinking component, this materialis preferably not added to the aqueous composition until just before thecomposition is applied to the substrate to be coated. This avoidspremature gelation or hardening of the composition over periods ofstorage.

The aqueous coating compositions of the invention will generally containfrom about 40 to about 85% by weight of liquid carrier, i.e., water or amixture of primarily water and water miscible organic solvents presentin the water dispersible polymer, with the balance of the formulationbeing polymer solids, unsaturated monomers, pigment, wetting agents andthe other ingredients which may be present in the composition. Theviscosity of the composition may be adjusted either by further dilutionwith water or by the addition of thickening agents to provide paintviscosities appropriate for the particular method of application to thesubstrate, e.g., brush, roller, pressure pot spray or airless spray.

The composition may be applied to the substrate at a dry thickness offrom about 0.5 to about 6 mils, preferably from about 2 to about 4 mils,by any suitable means such as spraying, brushing, roller coating and thelike. After application, the coated substrate is permitted to dry atambient temperatures, e.g., 20° to 35° C. The coating is normally dry tothe touch and tack free in less than 5 minutes, generally in 2 to 3minutes. Where the coating contains a cross linking agent activated byheat, it may be necessary to bake the coated substrate at temperaturesabove 100° C. to cure the coating.

Substrates which may be coated include cellulose and polymericsubstrates which contain active hydrogen in the polymer molecules. Suchsubstrates include wooden articles such as panels, window frames,flooring, siding and decorative articles such as shutters. Preshapedarticles made from polymers such as nylon or polypropylene may alsoserve as suitable substrates.

The coatings of the present invention offer numerous advantages overconventional protective coatings. They are free of hydrocarbon solventsexcept for organics such as ethers and esters and water miscible organoamine solvents which are present as impurities or carriers for thevarious components. This offers obvious environmental and safetyadvantages. The dried coatings are extremely durable and water resistantdue to the hydrophobic properties of the crosslinked coatings and impartUV resistance, abrasion resistance and anti-mildew, anti-fungicide andanti-spalling properties to the underlying substrate.

The following examples illustrate coating compositions which aresuitable for use in the present invention. Components used in theseformulations are as follows:

CYDROTHANE HP™ is a polyurethane-polyester polymer aqueous dispersionbased on an aliphatic diisocyante and containing carboxy/hydroxyfunctionality marketed by American Cyanamide Co. having a total solidscontent of 35% resin and a pH in the range of 9.5-10.0.

MAINCOTE™ AE-58 is a hydroxy functional acrylic resin aqueous dispersionavailable from Rohm and Haas Co. having a total solids content of 42.5%resin and a pH of 7.5.

SPENSOL™ L-51 is a carboxy-functional polyurethane dispersion availablefrom Textron, Inc. having a solids content of 30% by weight and a pH of8.5.

NEOCRYL™ A-612 is an aqueous acrylic emulsion containing carboxyfunctionality marketed by Polyvinyl Chemical Industries having a totalsolids content of 32% by weight, a pH of 7.7 and a content of naphta andalkoxy polyols of about 14% by weight.

NEOREZ™ R-960 is a polyurethane dispersion in N-methyl pyrrolidone andwater having a total solids content of 33% by weight, a pH of 8.3 and anacid number on solids of 30.

CX-100™ is a polyfunctional aziridine liquid crosslinking agent marketedby ICI Resins U.S., Inc.

Other components present in the formulations are identified by tradenameat first occurrence in the examples. These are well known materials suchas surfactants, pigments, wetting agents, flatting agents, flow controlagents, viscosity control additives (thickeners) and the like which areused in paint formulations.

These formations were prepared by placing the indicated quantity ofpolymer dispersion into a laboratory mixer and mixing in the monomers,pigments, peroxide, silver nitrate initiator and other ingredients setforth in examples I-VI.

EXAMPLE I

    ______________________________________                                                              PARTS BY                                                                      WEIGHT                                                  ______________________________________                                        CYDROTHANE ™ HP      60.00                                                 Titanium dioxide slurry (TIPURE ™ 742)                                                             20.00                                                 Ethoxylated Trimethylol Propane                                                                       0.50                                                  triacrylate                                                                   Polyethylene glycol (400) diacrylate                                                                  0.50                                                  Polyaziridine cross linker (CX-100)                                                                   0.70                                                  Acrylic Thickening Agent (ZIOTHIX ™ 96)                                                            3.00                                                  Urea peroxide 1% solution in water                                                                    0.10                                                  Silver nitrate 0.1% solution in water                                                                 0.10                                                  ______________________________________                                    

EXAMPLE II

    ______________________________________                                                                PARTS BY                                                                      WEIGHT                                                ______________________________________                                        MAINCOTE ™ 58          50.00                                               CYDROTHANE ™ HP        50.00                                               40) emulsion (POLY EM ™                                                                              6.00                                                Wax dispersion (SLIP-AYD ™ SL-300)                                                                   10.00                                               Titanium dioxide slurry   5.00                                                Titanium dioxide acrylic dispersion                                                                     15.00                                               (TINT-AYD ™ WD2002)                                                        Acrylic thickener (ACRYSOL ™ ASE-60)                                                                 0.75                                                Ammonia/water solution (1:1)                                                                            3.75                                                Fluorosurfactant (AQUA BEAD ™ 418E)                                                                  5.00                                                Hydroxy ethyl acrylate    0.50                                                Polyethylene glycol dimethacrylate                                                                      0.50                                                Urea peroxide 1% solution in water                                                                      0.10                                                Silver nitrate 0.1% solution in water                                                                   0.10                                                ______________________________________                                    

EXAMPLE III

    ______________________________________                                                                PARTS BY                                                                      WEIGHT                                                ______________________________________                                        CYDROTHANE ™ HP        100.00                                              Fluorosurfactant          5.00                                                Wax emulsion              5.00                                                Wax Dispersion            10.00                                               Titanium dioxide slurry   10.00                                               Titanium dioxide dispersion                                                                             10.00                                               Colloidal silica (CABOSPERSE ™ A-205)                                                                10.00                                               Ammonia/water solution (1:1)                                                                            13.00                                               341)siloxane wetting agent (BYK ™                                                                    1.00                                                Colloid thickener (ALCOGUM ™ 9440)                                                                   1.50                                                Polyaziridine cross linker                                                                              3.00                                                Ethoxylated trimethylol propane                                                                         0.50                                                triacylate                                                                    Polyethylene glycol (400) diacrylate                                                                    0.50                                                Urea peroxide 1% solution in water                                                                      0.10                                                Silver perchlorate 0.1% solution in water                                                               0.10                                                ______________________________________                                    

EXAMPLE IV

    ______________________________________                                                              PARTS BY                                                                      WEIGHT                                                  ______________________________________                                        SPENSOL ™ L-51       79.00                                                 CYDROTHANE ™ HP      10.00                                                 Deionized water         0.17                                                  Ammonium hydroxide      0.05                                                  Alkyd resin (AROLON ™ 860)                                                                         20.25                                                 Surfactant (SURFANOL ™ 104H)                                                                       0.66                                                  Wax dispersion          5.00                                                  Titanium dioxide slurry 10.00                                                 Fluorosurfactant        5.00                                                  Acrylic thickening agent                                                                              1.00                                                  Ammonia (28% aqueous sol.)                                                                            1.00                                                  Hydroxy ethyl acrylate  0.50                                                  Polypropylene glycol monomethacrylate                                                                 0.50                                                  Urea peroxide 1% solution in water                                                                    0.10                                                  Silver perchlorate 0.1% solution                                                                      0.10                                                  in water                                                                      ______________________________________                                    

EXAMPLE V

    ______________________________________                                                                PARTS BY                                                                      WEIGHT                                                ______________________________________                                        CYDROTHANE ™ HP        100.00                                              Fluorosurfactant          5.00                                                Wax emulsion              6.00                                                Wax dispersion            10.00                                               Titanium dioxide slurry   10.00                                               Titanium dioxide dispersion                                                                             10.00                                               Colloidal silica (CAB-O-SPERSE ™ A205)                                                               10.00                                               Polysiloxane wetting agent                                                                              1.00                                                Polyaziridine cross linker                                                                              0.50                                                NEOREZ ™ 960           5.00                                                Ethoxylated trimethylol propane                                                                         1.00                                                triacrylate                                                                   Polyethylene glycol (400) diacrylate                                                                    1.00                                                Polyethylene glycol dimethacrylate                                                                      0.50                                                Urea peroxide 1% solution in water                                                                      0.10                                                Silver nitrate 0.1% solution in water                                                                   0.10                                                ______________________________________                                    

EXAMPLE VI

    ______________________________________                                                                PARTS BY                                                                      WEIGHT                                                ______________________________________                                        NEOREZ ™ R-960         80.00                                               NEOCRYL ™ A 612        20.00                                               Titanium dioxide (UNITANE ™ 0-110)                                                                   10.00                                               Titanium dioxide dispersion                                                                             20.00                                               Surfactant (TRIONIC ™ 701)                                                                           10.00                                               Polyaziridine crosslinker  2.00                                               Polyethylene glycol (400) diacrylate                                                                     0.20                                               Ethoxylated trimethylol propane triacrylate                                                              0.20                                               Urea peroxide 1% solution in water                                                                       0.10                                               Silver nitrate 0.1% solution in water                                                                    0.10                                               ______________________________________                                    

Each of the formulations prepared in Examples I-VI were uniformlysprayed onto one surface of 12" by 12" unprimed wooden panels andpermitted to dry at about 32° C. for about 5 minutes. All samplescontaining polyaziridine crosslinker were essentially tack-free afterabout 2-3 minutes. All coatings were found to be well adhered to theunderlying wooden surface as reflected by an inability to scratch offthe coating from the wooden surface with a pencil tip.

The following example illustrates the excellent weathering, moistureresistance and substrate adhesion properties of the coating formulationsof the present invention.

EXAMPLE VII

Immediately after formulation, the coating composition of example VI wasuniformly sprayed onto the various surfaces of unprimed wooden panels toform sets as described below, and dried at 32° C. for five minutes. Thesamples were then aged at room temperature for several days. Finalcoating thickness was found to be in the order of 3-4 mils.

The coated wooden sets were as follows:

SET 1: Six (6) samples, 12"×13"×1/2" were coated on one 3"×12" face andnumbered Samples 1 through 6.

SET 2: Six (6) samples, 12"×3"×3/4" were coated on all sides and facesand numbered Samples 1 through 6.

SET 3: Six (6) samples, 16"×41/2"×3/8" were coated on one 16"×41/2" faceand numbered Samples 1 through 6.

The coated wooden samples were subjected to three testing procedures asfollows:

PROCEDURE 1

Samples 1 through 6 of Set 1 were subjected to accelerated weathering ingeneral accordance with ASTM E73-88, Standard Test Methods for SealDurability of Sealed Insulating Glass Units. The time of exposure wasfive weeks which was equivalent to 140 six-hour weather cycles.Evaluation of the specimens before and after weathering was performed inaccordance to ASTM-D523-89, Standard Test Method for Specular Gloss.

PROCEDURE 2

Samples 1 through 6 of Set 2 were tested in general accordance withASTDM D870-87, Standard Practice for Testing Water Resistance ofCoatings Using Water Immersion. The evaluation of the samples wasperformed as follows: Each sample was dried in a 150° F. convective ovenprior to immersion. The "dry" weight was then determined and recorded.The samples were then immersed in distilled water for 72 hours. At theconclusion of the immersion test, the "wet" weight was determined andrecorded. The percent absorption was calculated based on dry weight.

PROCEDURE 3

Samples 1 through 6 of Set 3 were tested in general accordance with ASTMD2486-89, Standard Test Method for Scrub Resistance of Interior LatexFlat Wall Paints. Evaluation was based on the number of scrub cyclesneeded to expose the bare wood.

Procedure 1 was performed on Step 1 in the weatherometer using anultra-violet light source over a five week period with the followingresults:

    ______________________________________                                                     Pre-Weathering                                                                            Post-Weathering                                      Samples No.  Gloss Reading                                                                             Gloss Reading                                        ______________________________________                                        1            30.8        27.7                                                 2            35.9        35.4                                                 3            31.2        21.0                                                 4            34.2        32.9                                                 5            39.0        36.8                                                 6            37.4        35.5                                                 ______________________________________                                    

All samples except for #3 exhibited a post-weathering gloss retention ofabout 90% or better. The surface appearance of all samples wasessentially unchanged at the conclusion of the test except that veryslight yellow streaking was observed on all samples after the 5 weekperiod. These results are also indicative of the resistance of thecoating to ultra-violet degradation.

Procedure 2 was performed on Set 2 over the 72 hour period with thefollowing results:

    ______________________________________                                               Pre-Immersion Post-Immersion                                           Samples                                                                              "Dry" Weight  "Wet" Weight                                                                              %                                            No.    (grams)       (grams)     Absorption                                   ______________________________________                                        1      207.13        211.82      2.26                                         2      198.15        239.00      20.26*                                       3      197.90        205.59      3.89                                         4      200.82        205.64      2.40                                         5      197.37        202.27      2.48                                         6      197.53        202.36      2.45                                         ______________________________________                                         *Note:                                                                        Sample No. 2 was observed to have voids in the coating exposing the           endgrain to direct contact with the water.                               

These test results demonstrate the excellent sealing properties andsubstrate adhesion properties of the formulations of the invention.Uncoated wood panels would absorb a minimum of 50 to 100% water at theconclusion of the test. The observation of only very slight yellowstreaking on the surfaces of all samples after 72 hours is indicative ofexcellent resistance to attack by mildew.

Procedure 3 was performed on Set 3. After exposure to 10,000 scrubcycles as described in ASTM D2486, Section 8, a definite area of wearwas observed in the scrub path of the brush, but no completewear-through to expose the underlying wooden surface was observed in anysample. These test results are indicative of the excellent hardness andabrasion resistance of the coatings of this invention as well asexcellent adhesion to the underlying wooden substrate.

What is claimed is:
 1. A coating composition in the form of an aqueousdispersion comprising a mixture of:a) a water dispersible polymerselected from the group consisting of acrylic polymers, urethanepolymers and mixtures thereof containing functional groups which arereactive under ambient conditions with a polyfunctional aziridinecrosslinking agent; b) at least one di or tri acrylate or methacrylateester; c) urea peroxide; d) silver nitrate; and e) a polyfunctionalaziridine crosslinking agent;said composition containing from about 75to about 95% by weight of component (a), on a dry weight basis; fromabout 0.05 to about 5% by weight of component (b); from about 0.0001 toabout 0.1% by weight of component (c); from about 0.0001 to about 0.01%by weight of component (d); and from about 1 to about 15% by weight ofcomponent (e) per 100 parts by weight of component (a), on a dry weightbasis.
 2. A coating composition in the form of an aqueous dispersioncomprising a mixture of:a) a water dispersible polymer selected from thegroup consisting of acrylic polymers, urethane polymers and mixturesthereof containing functional groups which are reactive under ambientconditions with a polyfunctional aziridine crosslinking agent; b) atleast one di or tri acrylate or methacrylate ester; c) urea peroxide;and d) silver nitrate; said composition containing from about 75 toabout 95% by weight of component (a), on a dry weight basis; from about0.05 to 5% by weight of component (b), from about 0.0001 to about 0.1%by weight of component (c); and from about 0.0001 to about 0.01% byweight of component (d).